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Self-administered Acupressure for Knee Osteoarthritis: A Pilot Randomized Controlled Trial

Primary Purpose

Knee Osteoarthritis

Status
Completed
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
Self-acupressure
Knee health education
Sponsored by
The Hong Kong Polytechnic University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Knee Osteoarthritis focused on measuring Knee Osteoarthritis

Eligibility Criteria

50 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • ethnic Chinese;
  • aged 50 -70 years
  • fulfills any 3 of the following criteria proposed by Altman et al., (1986): ( I. morning stiffness</= 30 min; ii. crepitus on active joint motion; iii. bone tenderness; iv. bone enlargement; or v. no palpable joint warmth);
  • having knee pain for at least 3 months;
  • ability to provide informed consent;
  • ability to comprehend Chinese; and
  • Knee pain ≥3/10 and </= 7 on a Likert pain scale from 1-10

Exclusion Criteria:

  • medical diagnoses or conditions that preclude individuals from active participation (bleeding disorders, alcohol or drug abuse);
  • presence of skin lesions or infections at the treatment sites;
  • currently participating in other interventional research studies for knee OA;
  • cognitive impairment preventing informed consent or understanding of instructions
  • body mass index over 25, the obese criteria for Asians (Anuurad et al., 2003);
  • knee pain related to other conditions (cancer, fracture, rheumatoid arthritis, rheumatism) as screened according to the red flags for further investigation or referral in the NICE 2014 Guidelines for Osteoarthritis of the knee;
  • had previous foot injury or trauma;
  • using of steroid for knee pain;
  • pregnancy or contemplating pregnancy;
  • ever received acupressure for knee OA over the past 6 months.

Sites / Locations

  • School of Nursing, the Hong Kong Polytechnic University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Self-acupressure Training

Knee Health Education

Arm Description

Subjects in the self-administered acupressure exercise group will receive two 1.5 hours acupressure training sessions. The training will be conducted in a group format with 4-7 subjects per group. Each subject will then receive a handout and an acupressure log. The handout includes a picture-illustrating acupressure step-by-step protocol. They will be told to perform the self-acupressure twice per day for 6 weeks.

Subjects in the health education control group will receive knowledge related to knee OA. The health education will be conducted in a talk format for 1.5 hours for two sessions.

Outcomes

Primary Outcome Measures

Pain severity numerical rating scale
A single 11-point numeric scale ranges from 0 to 10 in 1 cm intervals (zero: no pain, 10: greatest pain imaginable).

Secondary Outcome Measures

Western Ontario and McMaster University Osteoarthritis Index (WOMAC)
The Western and McMaster Universities Osteoarthritis Index (WOMAC, Likert version 3.1) covered pain, physical function, and stiffness related to knee osteoarthritis. The physical function subscale (consisting of 17 items) will be adopted to assess the level of physical function in patients with knee osteoarthritis under different activities.
Range of motion (ROM)
Range of motion is recorded in degrees by using a goniometer. ROM can be used to address the inter-relationship between ROMs of joint action and disability in patient with knee OA.
Short Form 6D (SF-6D)
The Short Form -6D is a preference-based measure of health derived from a selection of SF-36 items for economic evaluation.

Full Information

First Posted
May 14, 2017
Last Updated
September 21, 2023
Sponsor
The Hong Kong Polytechnic University
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1. Study Identification

Unique Protocol Identification Number
NCT03155737
Brief Title
Self-administered Acupressure for Knee Osteoarthritis: A Pilot Randomized Controlled Trial
Official Title
Self-administered Acupressure for Knee Osteoarthritis in Middle- and Older Adults: A Pilot Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Completed
Study Start Date
June 1, 2017 (Actual)
Primary Completion Date
October 31, 2017 (Actual)
Study Completion Date
March 31, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Hong Kong Polytechnic University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Objectives: To test the feasibility of the study design and clinical effects of self-administered acupressure on relieving knee osteoarthritis (OA) pain. Hypothesis: self-administered acupressure would have a superior beneficial effect compared to health education control group in terms of pain relief in patients with knee osteoarthritis across the 6-week study period. Design and subjects: A pilot randomized controlled trial. 36 subjects with knee OA will be recruited; 18 per group. All eligible subjects will be randomized to either self-administered acupressure or health education control group in 1:1 ratio. Interventions: Subjects in the self-acupressure group will attend two 1.5 hours training sessions to learn self-acupressure and will practice self-acupressure every morning and night for 6 weeks; subjects in the education control group will receive two 1.5 hours training sessions to learn the health information related to knee OA. Main outcome measures: The primary outcome measure is the numerical rating scale for knee pain. Other measures include Western Ontario and McMaster University Osteoarthritis Index, knees' range of motion (ROM), and SF-6D. Acceptability of the self-acupressure training course will also be evaluated. Data Analysis: Differences in the questionnaire scores and ROM will be examined using a mixed-effects model. Both completer and intention-to-treat analyses will be conducted. Effect sizes will be computed by dividing the difference in means by the pooled standard deviation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Knee Osteoarthritis
Keywords
Knee Osteoarthritis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
35 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Self-acupressure Training
Arm Type
Experimental
Arm Description
Subjects in the self-administered acupressure exercise group will receive two 1.5 hours acupressure training sessions. The training will be conducted in a group format with 4-7 subjects per group. Each subject will then receive a handout and an acupressure log. The handout includes a picture-illustrating acupressure step-by-step protocol. They will be told to perform the self-acupressure twice per day for 6 weeks.
Arm Title
Knee Health Education
Arm Type
Active Comparator
Arm Description
Subjects in the health education control group will receive knowledge related to knee OA. The health education will be conducted in a talk format for 1.5 hours for two sessions.
Intervention Type
Other
Intervention Name(s)
Self-acupressure
Intervention Description
A training course will be offered to subjects in this group to train them to perform self-acupressure.
Intervention Type
Other
Intervention Name(s)
Knee health education
Intervention Description
A course regarding knee health will be offered to the subjects in this group.
Primary Outcome Measure Information:
Title
Pain severity numerical rating scale
Description
A single 11-point numeric scale ranges from 0 to 10 in 1 cm intervals (zero: no pain, 10: greatest pain imaginable).
Time Frame
Week 6
Secondary Outcome Measure Information:
Title
Western Ontario and McMaster University Osteoarthritis Index (WOMAC)
Description
The Western and McMaster Universities Osteoarthritis Index (WOMAC, Likert version 3.1) covered pain, physical function, and stiffness related to knee osteoarthritis. The physical function subscale (consisting of 17 items) will be adopted to assess the level of physical function in patients with knee osteoarthritis under different activities.
Time Frame
Baseline, Week 2, Week 4, Week 6
Title
Range of motion (ROM)
Description
Range of motion is recorded in degrees by using a goniometer. ROM can be used to address the inter-relationship between ROMs of joint action and disability in patient with knee OA.
Time Frame
Baseline, Week 6
Title
Short Form 6D (SF-6D)
Description
The Short Form -6D is a preference-based measure of health derived from a selection of SF-36 items for economic evaluation.
Time Frame
Baseline, Week 6

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: ethnic Chinese; aged 50 -70 years fulfills any 3 of the following criteria proposed by Altman et al., (1986): ( I. morning stiffness</= 30 min; ii. crepitus on active joint motion; iii. bone tenderness; iv. bone enlargement; or v. no palpable joint warmth); having knee pain for at least 3 months; ability to provide informed consent; ability to comprehend Chinese; and Knee pain ≥3/10 and </= 7 on a Likert pain scale from 1-10 Exclusion Criteria: medical diagnoses or conditions that preclude individuals from active participation (bleeding disorders, alcohol or drug abuse); presence of skin lesions or infections at the treatment sites; currently participating in other interventional research studies for knee OA; cognitive impairment preventing informed consent or understanding of instructions body mass index over 25, the obese criteria for Asians (Anuurad et al., 2003); knee pain related to other conditions (cancer, fracture, rheumatoid arthritis, rheumatism) as screened according to the red flags for further investigation or referral in the NICE 2014 Guidelines for Osteoarthritis of the knee; had previous foot injury or trauma; using of steroid for knee pain; pregnancy or contemplating pregnancy; ever received acupressure for knee OA over the past 6 months.
Facility Information:
Facility Name
School of Nursing, the Hong Kong Polytechnic University
City
Hong Kong
Country
Hong Kong

12. IPD Sharing Statement

Plan to Share IPD
No

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Self-administered Acupressure for Knee Osteoarthritis: A Pilot Randomized Controlled Trial

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